Informaţii despre

Nume Blood Coagulation Disease
Pagina Web www.malacards.org
Clasificari ICD10 Coagulation defect, unspecified; Postpartum coagulation defects
Clasificare anatomică Malacards Boli de sânge
Boli din aceeaşi familie Inherited Blood Coagulation Disease

Vezi şi

Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acquired Von Willebrand Syndrome Acute Leukemia Acute Liver Failure Acute Maxillary Sinusitis Acute Myocardial Infarction Afibrinogenemia Afibrinogenemia, Congenital Alcohol-Related Birth Defect Alpha-2-Plasmin Inhibitor Deficiency Al-Raqad Syndrome Amaurosis Fugax Amegakaryocytic Thrombocytopenia, Congenital Angina Pectoris Aniridia 1 Anomalous Left Coronary Artery from the Pulmonary Artery Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterior Spinal Artery Syndrome Anteroseptal Myocardial Infarction Antiphospholipid Syndrome Antithrombin Iii Deficiency Arteriosclerosis Arteriosclerosis Obliterans Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Autoimmune Disease of Blood Autosomal Dominant Macrothrombocytopenia Basilar Artery Occlusion Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Bleeding Disorder, Platelet-Type, 16 Blood Group--Ahonen Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Bombay Phenotype Bone Marrow Cancer Branch Retinal Artery Occlusion Budd-Chiari Syndrome Buerger Disease Caffey Disease Cardiac Tamponade Carotid Artery Dissection Carotid Artery Occlusion Carotid Artery Thrombosis Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Cerebral Arteritis Cerebral Falx Meningioma Cerebral Palsy Cerebral Sinovenous Thrombosis Cold Urticaria Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Ia Conjugate Gaze Palsy Coronary Thrombosis Cryptogenic Cirrhosis Dengue Hemorrhagic Fever Diabetic Angiopathy Disseminated Intravascular Coagulation Dysbaric Osteonecrosis Dysfibrinogenemia Dyskeratosis Congenita, Autosomal Dominant 6 Eclampsia Endocardium Disease Esophageal Varix Essential Thrombocythemia Evans' Syndrome Exanthema Subitum Factor V and Factor Viii, Combined Deficiency of, 2 Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Femoral Neuropathy Fetal and Neonatal Alloimmune Thrombocytopenia Fournier Gangrene Giant Hemangioma Glanzmann Thrombasthenia Gray Platelet Syndrome Hantavirus Pulmonary Syndrome Hellp Syndrome Hemarthrosis Hemoglobin E Disease Hemolytic-Uremic Syndrome Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis a Hepatitis D Homocysteinemia Homocystinuria Hypersplenism Immune System Disease Infective Endocarditis Inferior Vena Cava Interruption Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Japanese Spotted Fever Korean Hemorrhagic Fever Lateral Myocardial Infarction Leech Infestation Legg-Calve-Perthes Disease Lemierre's Syndrome Livedoid Vasculopathy Liver Cirrhosis Malignant Dermis Tumor Malignant Skin Fibrous Histiocytoma Marantic Endocarditis Megakaryocytic Leukemia Meningococcemia Mesenteric Vascular Occlusion Mild Hemophilia a Mitral Valve Stenosis Monoclonal Paraproteinemia Myelofibrosis Nonarteritic Anterior Ischemic Optic Neuropathy Orbital Granuloma Osteonecrosis Osteosclerotic Myeloma Pancytopenia Paracetamol Poisoning Patent Foramen Ovale Peripheral Vertigo Placenta Disease Placental Abruption Platelet Aggregation, Spontaneous Polycythemia Polycythemia Vera Porencephaly Portal Hypertension Portal Vein Thrombosis Posterolateral Myocardial Infarction Post-Thrombotic Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Primary Thrombocytopenia Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pseudo-Von Willebrand Disease Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Raynaud Disease Refractory Anemia Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Sagittal Sinus Thrombosis Schizencephaly Scott Syndrome Severe Hemophilia a Severe Hemophilia B Sickle Cell Anemia Sneddon Syndrome Spinal Cord Infarction Splenic Disease Splenomegaly Spotted Fever Sticky Platelet Syndrome Stroke, Ischemic Sudden Sensorineural Hearing Loss Syphilitic Meningitis Takayasu Arteritis Thrombasthenia Thrombocythemia 1 Thrombocytopenia Thrombocytopenia 3 Thrombocytopenia-Absent Radius Syndrome Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Unilateral Absence of a Pulmonary Artery Varicose Veins Vasculitis Vein Disease Velocardiofacial Syndrome Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Von Willebrand Disease, Type 3